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3-(Prop-2-enylamino)propanenitrile, also known as allyl glycidyl cyanide, is an organic compound with the chemical formula C6H8N2. It is a colorless liquid with a pungent odor and is soluble in water. 3-(prop-2-enylamino)propanenitrile is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its potential use as a monomer in the production of polymers. Due to its reactivity, it is important to handle this chemical with care, as it can be toxic and may cause irritation to the skin, eyes, and respiratory system.

34508-81-1

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34508-81-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 34508-81-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,5,0 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34508-81:
(7*3)+(6*4)+(5*5)+(4*0)+(3*8)+(2*8)+(1*1)=111
111 % 10 = 1
So 34508-81-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H10N2/c1-2-5-8-6-3-4-7/h2,8H,1,3,5-6H2

34508-81-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(prop-2-enylamino)propanenitrile

1.2 Other means of identification

Product number -
Other names 3-Allylamino-propionsaeure-nitril

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:34508-81-1 SDS

34508-81-1Downstream Products

34508-81-1Relevant academic research and scientific papers

6-MEMBERED URACIL ISOSTERES

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Paragraph 0819, (2018/06/12)

Provided herein are dUTPase inhibitors, compositions comprising such compounds and methods of using such compounds and compositions.

AMINO SULFONYL COMPOUNDS

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Paragraph 0533, (2018/06/12)

Provided herein are dUTPase inhibitors, compositions comprising such compounds and methods of using such compounds and compositions.

URACIL CONTAINING COMPOUNDS

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Paragraph 0754, (2018/07/31)

Provided herein are dUTPase inhibitors, compositions comprising such compounds and methods of using such compounds and compositions.

Synthesis and Structure of [Cu(Hapn)]NO3]NO3, [Cu(Hapn)(H2O)2]SiF6, [Cu(Hapn)(H2O)BF4]BF4 · H2O and [Cu(Hapn)(NH2SO3)2] π-complexes (apn = 3-(prop-2-en-1-ylamino)propanenitrile)

Luk'Yanov, Mykhailo,Goreshnik, Evgeny,Kinzhybalo, Vasyl,Mys'kiv, Marian

, p. 208 - 214 (2017/04/01)

Four copper(I) π-complexes: [Cu(Hapn)NO3]NO3 (1), [Cu(Hapn)(H2O)2]SiF6 (2), [Cu(Hapn)(H2O)BF4]BF4·H2O (3) and [Cu(Hapn)(NH2SO3)2] (4) were prepared using alternating-current electrochemical technique, starting from alcohol solutions of 3-(prop-2-en-1-ylamino)propanenitrile (apn) titrated with appropriate acid and copper(II) salts (Cu(NO3)2 · 3H2O, CuSiF6 · 4H2O, Cu(BF4)2 · 6H2O or Cu(NH2SO3)2 · xH2O, respectively). Obtained compounds were characterized by single-crystal X-ray diffraction and partially by IR spectroscopy. In the structures of complexes 1, 2 and 4 Cu(I) cation possesses a tetrahedral environment formed by the C=C bond of one organic cation Hapn, the N atom of cyano group from another Hapn moiety, and two O atoms (from NO3- anions in 1, from H2O molecules in 2) or N atoms (NH2SO3- anions in 4). In compound 3 strongly pronounced trigonal-pyramidal coordination environment of Cu(I) is formed by a mid-point of C=C-bond of one Hapn cation, nitrogen atom (of cyano group) of another Hapn unit, O atom of H2O molecule in the basal plane, and F atom of BF4- anion at the apical position.

DEOXYURIDINE TRIPHOSPHATASE INHIBITORS

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Paragraph 0400-0401, (2017/01/26)

Provided herein are dUTPase inhibitors, compositions comprising such compounds and methods of using such compounds and compositions.

DEOXYURIDINE TRIPHOSPHATASE INHIBITORS CONTAINING CYCLOPROPANO LINKAGE

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Paragraph 0370; 0371, (2017/02/09)

Provided herein are dUTPase inhibitors, compositions comprising such compounds and methods of using such compounds and compositions.

Synthesis and biological evaluation of tetrahydropyridinepyrazoles ('PFPs') as inhibitors of STAT3 phosphorylation

Revanna,Srinivasa,Li, Feng,Siveen, Kodappully Sivaraman,Dai, Xiaoyun,Swamy, Shivananju Nanjunda,Bhadregowda,Sethi, Gautam,Mantelingu,Bender, Andreas,Ks, Rangappa

supporting information, p. 32 - 40 (2014/01/06)

The transcription factor STAT3 is constitutively overexpressed in many human tumors and hence represents a putative target for anticancer drug design. In this work, we describe the synthesis and biological evaluation of a novel chemotype, pyridine-fused p

Convenient synthesis of novel N-(5-allyl-7,7-difluoro)-4,5,6,7-tetrahydro- 2H-indazol-3-yl)-carboxymides

Revanna, Chigalli N.,Raghavendra, Goravanahalli M.,Nandeesh, Kebbahalli N.,Bhadregowda, Doddamedur G.,Rangappa, Kanchugarakoppal S.,Mantelingu, Kempegowda

supporting information, p. 5224 - 5226 (2013/09/02)

5-Allyl-7,7-difluoro-2-(2,4-difluorophenyl)-6-(4-methoxyphenyl)-4,5,6, 7-tetrahydro-2H-pyrazolo[4,3-c]pyridine-3-amine represents a fluorinated heterocyclic scaffold, potentially attractive. It was synthesized via Michael addition, Mannich reaction of the

π-Complexes of copper(I) halides with 3-(allylamino)-(C3H 5NHC2H4CN, Apn) and 3-(diallylamino)-((C3H 5)2NC2H4CN, dapn)-propanenitrile. Syntheses and crystal structures of compounds [CuCl(Apn)], [(H+Apn)Cu2Cl 3], [(H+dapn)CuCl2], and [(H+dapn)CuBr2]

Luk'yanov,Pavlyuk,Mys'kiv

experimental part, p. 86 - 91 (2012/07/14)

The π-complexes [CuCl(C3H5NHC2H4CN)] (I), [(C 3H5NH2C2H4CN)Cu2Cl3] (II), [((C3H5)2NHC2H 4CN)CuCl2] (III), and [((C3H5)2NHC2H4CN)CuBr2] (IV) are obtained as single crystals by the ac electrochemical synthesis on copper wire electrodes from ethanolic solutions of 3-(allylamino)propanenitrile, 3-(diallylamino)propanenitrile, and CuX2 (X = Cl, Br). Their crystal structures are determined. The crystals of compounds I, III, and IV are monoclinic, space group P21/c, Z = 4. The crystals of compound II are triclinic, space group P1, Z = 2. The unit cell parameters are a = 11.125(4), b = 8.769(4), c = 8.570(4) A, β = 90.94(4)°, V = 835.9(6) A3 (I); a = 6.2566(4), b = 7.5975(6), c = 11.1251(8) A, α = 90.896(6)°, β = 92.827(5)°, γ = 94.340(5)°, V = 526.57(7) A3 (II); a= 11.656(4), b= 6.992(4), c = 14.681(5) A, β = 100.89(4)°, V = 1174.9(9) A3 (III); a = 11.845(4), b = 7.282(4), c= 14.855(5) A, β = 100.37(4)°, V = 1260.4(9) A3 (IV). The coordination mode of the Cu(I) atom in complex I includes two halogen atoms, the C=C bond, and the secondary amine N atom. The coordination environment in isostructural crystals of complexes III and IV is formed by the C=C bond and three halogen atoms as in complex II. Pleiades Publishing, Ltd., 2012.

A one-pot, three-component synthesis of thiazolidine-2-thiones

Ziyaei-Halimehjani, Azim,Marjani, Katayoun,Ashouri, Akram

body text, p. 3490 - 3492 (2012/08/27)

An efficient method for the synthesis of thiazolidine-2-thiones is described via regiospecific iodocyclization of an allyl amine, carbon disulfide, and iodine. Dehydrohalogenation of the iodo-derivatives gives thiazole-2(3H)-thiones. In addition, nucleoph

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